EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS173-15188 
Organism
Homo sapiens 
Tissue/cell
SH-SY5Y 
Coordinate
chr9:134608500-134609980 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GATA2MA0036.3chr9:134609391-134609402TTCTTATCTCT+6.32
Gata1MA0035.3chr9:134609391-134609402TTCTTATCTCT+6.32
Gata4MA0482.1chr9:134609392-134609403TCTTATCTCTC+6.32
JUN(var.2)MA0489.1chr9:134609237-134609251ATGACTCATCTCTA-6.08
RREB1MA0073.1chr9:134608753-134608773GGGGGGGGGGTGGTGCGGGG-7.56
ZNF740MA0753.2chr9:134608753-134608766GGGGGGGGGGTGG-6.44
Number of super-enhancer constituents: 41             
IDCoordinateTissue/cell
SE_00686chr9:134608884-134613190Adipose_Nuclei
SE_04525chr9:134608863-134612853Brain_Anterior_Caudate
SE_09150chr9:134602020-134613269CD14
SE_10404chr9:134599070-134613095CD19_Primary
SE_10884chr9:134591844-134615384CD20
SE_12120chr9:134606082-134613193CD3
SE_14804chr9:134606083-134613399CD4_Memory_Primary_7pool
SE_16701chr9:134601791-134611990CD4_Naive_Primary_8pool
SE_17150chr9:134606063-134613218CD4p_CD225int_CD127p_Tmem
SE_17952chr9:134601452-134615329CD4p_CD25-_CD45ROp_Memory
SE_18769chr9:134601534-134615309CD4p_CD25-_Il17-_PMAstim_Th
SE_19472chr9:134602036-134615436CD4p_CD25-_Il17p_PMAstim_Th17
SE_20363chr9:134601294-134613216CD56
SE_22914chr9:134601848-134613223CD8_primiary
SE_27117chr9:134606526-134611391Esophagus
SE_30786chr9:134606415-134610798Fetal_Muscle
SE_31710chr9:134608376-134613068Gastric
SE_32578chr9:134599803-134613266GM12878
SE_33628chr9:134605461-134610903H2171
SE_36750chr9:134606498-134610470HMEC
SE_36915chr9:134602036-134616473HSMMtube
SE_38234chr9:134607748-134613138HUVEC
SE_40722chr9:134606610-134608765Left_Ventricle
SE_40722chr9:134608773-134610234Left_Ventricle
SE_42566chr9:134606682-134613188Lung
SE_44033chr9:134608797-134610392MM1S
SE_49262chr9:134608245-134611154Right_Atrium
SE_50405chr9:134606039-134613162Sigmoid_Colon
SE_52037chr9:134606112-134612282Skeletal_Muscle_Myoblast
SE_52732chr9:134605999-134613197Small_Intestine
SE_54202chr9:134601963-134613163Spleen
SE_58352chr9:134520171-134620333Ly1
SE_58881chr9:134579557-134620273Ly3
SE_60383chr9:134599961-134620084Ly4
SE_60991chr9:134494570-134620113HBL1
SE_61989chr9:134594251-134616125Toledo
SE_62218chr9:134495530-134621458Tonsil
SE_63796chr9:134606096-134612370HSMM
SE_64992chr9:134606662-134610348NHEK
SE_66603chr9:134606093-134608710Jurkat
SE_66603chr9:134608729-134612181Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr9134609553134609906
chr9134608936134609538
Enhancer Sequence
GGTCCAAGGA GGAGCCTCGG CCACAGCTAA GCAGGAAGGA CTGCATTCAA AGAGGCTTCC 60
CCATTAGTGG TTACCTAATG GCCTTCTTAT GTATAAAAAA GGGCCTGCAG TCACGCATGC 120
GGGGCTTCAA ACCTAGATGA CGGGTTGATA GGTGCAGCAA ACCGCCACGG CACATGTATA 180
CCTATGTAAC AAACCTGAAC GTTCAGCACA TGTATTCCAG AACTTAAAAT TTAAAAAAGC 240
CGGGGCGGGG GCGGGGGGGG GGGTGGTGCG GGGTTGGCGG GGGCAGTGGC TACAGCTTAA 300
AAACACAAAC AGAGGAGCGC TCCTTTTGAG TCCCACTCCT TCCTGGCACT GATGGGGAAA 360
ATAAGCCCCA GGAAAGGGTA AGAATCACCC AAGGACACAA CTAAGATGTT CTCAAACAGA 420
TGACCAGAAA CTAAGATGAC TGGCCTGCTG GATGACAGAT CCCTTAATAA TTCACAAACG 480
GTGGGTTTTA TTTATTTACT CATAAAACAG CCTTTGGGGC AAGACGGGTG ACGAGTCAGA 540
GGAACACCTG TCCCGGCGGC GAGGCGGCCG CGGGGTGGGG CAGGCGGTGG GTTGTCAGGC 600
CTCTCCTCTT TCCAGAGCGT GATCTTATCC TGGCCATGGG GAACACGCTC AGCTGGCCTG 660
AGGTAAGACC CAGCCTGGCA CTCAAGGCAA TCTCCAATCC GGGCTACTTT GGGAGACATT 720
TTTCTGCAAG CTCACACATG ACTCATCTCT ACAGACCTCC TATAAGGTCT CTTGGCTACA 780
AGGAATCCCA TTCAAACCGC CTCTGCCAAC AGCTGCTCTG GAGACCAGGA AACATTTGGG 840
GTTGCTGTGG TTGATTTTTC TAAAAACACA CTTAGCTGGC ATTAGTGCTA TTTCTTATCT 900
CTCTACAGCA CTGTTAATGT GACTAGTATT ACGAGTATCA GACGCAGTCT AAAGACTGTA 960
GTGAGCCTCC CTTAATTTCA TTGGTAGATC TTTTTTTTCA AAGATCAGAA AAGAGATTGA 1020
GAAGCCTGAA GAATTAAGAT GGAAAGCTGT GTCCCCAGCA ACCAGGGAGG CTCTAACCAG 1080
TGCTCTATAA AGGCAAGAAA GGGGGCCGGT TCCCCATTCC ACTTCTCCAG GGCATGACCT 1140
TGGGCAAACA ACCAAATTTC CCTGGGCCTT AGCTGCCCTG AGGGGCAAAA GAGGGATACT 1200
CCGCCCTGCC CTCACCCCCT GGGCTGTTGT GAGGATGAAA TGAAATGAGG TAGTCTATAA 1260
ATGCATTCTG AAAACCACAG GAAATTGCAG AGATGTTCAA GATCGTTCTG ATTCTACCCC 1320
TGGACTGTGG CCTCCAGGGA CAGGTTCCTG CTGGCTCCCT GCCACGAGGC ATCACTTGGT 1380
GTTTGCCAAC AAGGAGGCAC TCAGTAAGTG TTAAAACGGG TGAGTGAAAG GAGGCAGAGC 1440
AGGTGCCATC AAAATGTCTC ATTGCTTGAC TGAGTATACT 1480